JPH08508529A - 高耐衝撃性ポリエステル／ポリカーボネート・ブレンド - Google Patents

高耐衝撃性ポリエステル／ポリカーボネート・ブレンド

Info

Publication number: JPH08508529A
Authority: JP; Japan
Prior art keywords: poly; polycarbonate; polyester; blend; elastomer
Prior art date: 1993-04-05
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.): Pending

Application number

JP6522157A

Other languages

English (en)

Japanese (ja)

Inventor

アカペッディ，ムラリ・クリシュナ

バンバスカーク，ブルース

Original Assignee

アライドシグナル・インコーポレーテッド

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1993-04-05

Filing date

1994-03-23

Publication date

1996-09-10

1994-03-23 Application filed by アライドシグナル・インコーポレーテッド filed Critical アライドシグナル・インコーポレーテッド

1996-09-10 Publication of JPH08508529A publication Critical patent/JPH08508529A/ja

Status Pending legal-status Critical Current

Links

239000000203 mixture Substances 0.000 title claims abstract description 86
229920000728 polyester Polymers 0.000 title claims abstract description 66
229920000515 polycarbonate Polymers 0.000 title claims abstract description 61
239000004417 polycarbonate Substances 0.000 title claims abstract description 61
229920001971 elastomer Polymers 0.000 claims abstract description 58
239000000806 elastomer Substances 0.000 claims abstract description 49
239000007822 coupling agent Substances 0.000 claims abstract description 25
150000001412 amines Chemical class 0.000 claims abstract description 15
-1 4-hydroxy-3,5-dimethylphenyl Chemical group 0.000 claims description 27
238000000034 method Methods 0.000 claims description 27
229920000139 polyethylene terephthalate Polymers 0.000 claims description 22
239000005020 polyethylene terephthalate Substances 0.000 claims description 22
229920001577 copolymer Polymers 0.000 claims description 18
KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 claims description 14
125000003277 amino group Chemical group 0.000 claims description 12
238000002156 mixing Methods 0.000 claims description 9
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Natural products C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 8
HQQADJVZYDDRJT-UHFFFAOYSA-N ethene;prop-1-ene Chemical group C=C.CC=C HQQADJVZYDDRJT-UHFFFAOYSA-N 0.000 claims description 8
229920001169 thermoplastic Polymers 0.000 claims description 7
239000004416 thermosoftening plastic Substances 0.000 claims description 7
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 6
239000005977 Ethylene Substances 0.000 claims description 6
150000001718 carbodiimides Chemical class 0.000 claims description 6
150000001993 dienes Chemical class 0.000 claims description 6
229920002959 polymer blend Polymers 0.000 claims description 6
VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical group CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 claims description 4
150000001335 aliphatic alkanes Chemical class 0.000 claims description 4
125000002947 alkylene group Chemical group 0.000 claims description 4
150000004649 carbonic acid derivatives Chemical class 0.000 claims description 4
229920001897 terpolymer Polymers 0.000 claims description 4
238000004519 manufacturing process Methods 0.000 claims description 3
229920001707 polybutylene terephthalate Polymers 0.000 claims description 3
229920000800 acrylic rubber Polymers 0.000 claims description 2
238000007334 copolymerization reaction Methods 0.000 claims description 2
229920006228 ethylene acrylate copolymer Polymers 0.000 claims description 2
229920000578 graft copolymer Polymers 0.000 claims description 2
229920001195 polyisoprene Polymers 0.000 claims description 2
KKEYFWRCBNTPAC-UHFFFAOYSA-L terephthalate(2-) Chemical compound [O-]C(=O)C1=CC=C(C([O-])=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-L 0.000 claims description 2
125000004203 4-hydroxyphenyl group Chemical group [H]OC1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 1
239000005062 Polybutadiene Substances 0.000 claims 1
125000000217 alkyl group Chemical group 0.000 claims 1
125000000732 arylene group Chemical group 0.000 claims 1
NTXGQCSETZTARF-UHFFFAOYSA-N buta-1,3-diene;prop-2-enenitrile Chemical compound C=CC=C.C=CC#N NTXGQCSETZTARF-UHFFFAOYSA-N 0.000 claims 1
125000002993 cycloalkylene group Chemical group 0.000 claims 1
229920002857 polybutadiene Polymers 0.000 claims 1
229920000642 polymer Polymers 0.000 description 21
239000002253 acid Substances 0.000 description 10
230000000052 comparative effect Effects 0.000 description 10
239000008188 pellet Substances 0.000 description 10
239000000843 powder Substances 0.000 description 10
238000002474 experimental method Methods 0.000 description 9
239000005060 rubber Substances 0.000 description 9
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 8
125000004432 carbon atom Chemical group C* 0.000 description 8
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 8
239000000178 monomer Substances 0.000 description 8
238000000465 moulding Methods 0.000 description 8
OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 7
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 7
238000000137 annealing Methods 0.000 description 7
125000003118 aryl group Chemical group 0.000 description 7
150000002009 diols Chemical class 0.000 description 7
239000004615 ingredient Substances 0.000 description 7
238000001746 injection moulding Methods 0.000 description 7
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
229920004142 LEXAN™ Polymers 0.000 description 5
239000004418 Lexan Substances 0.000 description 5
150000007513 acids Chemical class 0.000 description 5
125000001931 aliphatic group Chemical group 0.000 description 5
238000010438 heat treatment Methods 0.000 description 5
239000000047 product Substances 0.000 description 5
WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 4
238000001125 extrusion Methods 0.000 description 4
239000012948 isocyanate Substances 0.000 description 4
150000002513 isocyanates Chemical class 0.000 description 4
239000000463 material Substances 0.000 description 4
230000000717 retained effect Effects 0.000 description 4
239000002904 solvent Substances 0.000 description 4
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 3
ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 3
KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 3
239000003054 catalyst Substances 0.000 description 3
239000003795 chemical substances by application Substances 0.000 description 3
238000009833 condensation Methods 0.000 description 3
230000005494 condensation Effects 0.000 description 3
150000001991 dicarboxylic acids Chemical class 0.000 description 3
125000000524 functional group Chemical group 0.000 description 3
239000000155 melt Substances 0.000 description 3
238000002844 melting Methods 0.000 description 3
230000008018 melting Effects 0.000 description 3
229910052698 phosphorus Inorganic materials 0.000 description 3
239000011574 phosphorus Substances 0.000 description 3
XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 3
239000002243 precursor Substances 0.000 description 3
150000003254 radicals Chemical class 0.000 description 3
239000000126 substance Substances 0.000 description 3
238000012360 testing method Methods 0.000 description 3
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
YGYNBBAUIYTWBF-UHFFFAOYSA-N 2,6-dimethylnaphthalene Chemical compound C1=C(C)C=CC2=CC(C)=CC=C21 YGYNBBAUIYTWBF-UHFFFAOYSA-N 0.000 description 2
ZPJDFKVKOFGAFV-UHFFFAOYSA-N 2-octadecylbutanedioic acid Chemical compound CCCCCCCCCCCCCCCCCCC(C(O)=O)CC(O)=O ZPJDFKVKOFGAFV-UHFFFAOYSA-N 0.000 description 2
PLIKAWJENQZMHA-UHFFFAOYSA-N 4-aminophenol Chemical compound NC1=CC=C(O)C=C1 PLIKAWJENQZMHA-UHFFFAOYSA-N 0.000 description 2
NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 2
QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 2
OWYWGLHRNBIFJP-UHFFFAOYSA-N Ipazine Chemical compound CCN(CC)C1=NC(Cl)=NC(NC(C)C)=N1 OWYWGLHRNBIFJP-UHFFFAOYSA-N 0.000 description 2
UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 2
BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 description 2
229920000459 Nitrile rubber Polymers 0.000 description 2
KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 2
YIMQCDZDWXUDCA-UHFFFAOYSA-N [4-(hydroxymethyl)cyclohexyl]methanol Chemical compound OCC1CCC(CO)CC1 YIMQCDZDWXUDCA-UHFFFAOYSA-N 0.000 description 2
239000000853 adhesive Substances 0.000 description 2
230000001070 adhesive effect Effects 0.000 description 2
WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
125000002723 alicyclic group Chemical group 0.000 description 2
230000015572 biosynthetic process Effects 0.000 description 2
IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 2
HQABUPZFAYXKJW-UHFFFAOYSA-N butan-1-amine Chemical compound CCCCN HQABUPZFAYXKJW-UHFFFAOYSA-N 0.000 description 2
150000001732 carboxylic acid derivatives Chemical group 0.000 description 2
238000006243 chemical reaction Methods 0.000 description 2
IYYZUPMFVPLQIF-UHFFFAOYSA-N dibenzothiophene Chemical compound C1=CC=C2C3=CC=CC=C3SC2=C1 IYYZUPMFVPLQIF-UHFFFAOYSA-N 0.000 description 2
QDOXWKRWXJOMAK-UHFFFAOYSA-N dichromium trioxide Chemical compound O=[Cr]O[Cr]=O QDOXWKRWXJOMAK-UHFFFAOYSA-N 0.000 description 2
KZTYYGOKRVBIMI-UHFFFAOYSA-N diphenyl sulfone Chemical compound C=1C=CC=CC=1S(=O)(=O)C1=CC=CC=C1 KZTYYGOKRVBIMI-UHFFFAOYSA-N 0.000 description 2
CZZYITDELCSZES-UHFFFAOYSA-N diphenylmethane Chemical compound C=1C=CC=CC=1CC1=CC=CC=C1 CZZYITDELCSZES-UHFFFAOYSA-N 0.000 description 2
GHLKSLMMWAKNBM-UHFFFAOYSA-N dodecane-1,12-diol Chemical compound OCCCCCCCCCCCCO GHLKSLMMWAKNBM-UHFFFAOYSA-N 0.000 description 2
230000000694 effects Effects 0.000 description 2
238000005516 engineering process Methods 0.000 description 2
JBKVHLHDHHXQEQ-UHFFFAOYSA-N epsilon-caprolactam Chemical group O=C1CCCCCN1 JBKVHLHDHHXQEQ-UHFFFAOYSA-N 0.000 description 2
229920001519 homopolymer Polymers 0.000 description 2
125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
238000002347 injection Methods 0.000 description 2
239000007924 injection Substances 0.000 description 2
QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 2
238000010128 melt processing Methods 0.000 description 2
VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
JFNLZVQOOSMTJK-KNVOCYPGSA-N norbornene Chemical compound C1[C@@H]2CC[C@H]1C=C2 JFNLZVQOOSMTJK-KNVOCYPGSA-N 0.000 description 2
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
239000001294 propane Substances 0.000 description 2
QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 2
125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 2
CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 2
239000000243 solution Substances 0.000 description 2
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TYFQFVWCELRYAO-UHFFFAOYSA-N suberic acid Chemical compound OC(=O)CCCCCCC(O)=O TYFQFVWCELRYAO-UHFFFAOYSA-N 0.000 description 2
150000003457 sulfones Chemical class 0.000 description 2
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PORWMNRCUJJQNO-UHFFFAOYSA-N tellurium atom Chemical compound [Te] PORWMNRCUJJQNO-UHFFFAOYSA-N 0.000 description 2
HVLLSGMXQDNUAL-UHFFFAOYSA-N triphenyl phosphite Chemical compound C=1C=CC=CC=1OP(OC=1C=CC=CC=1)OC1=CC=CC=C1 HVLLSGMXQDNUAL-UHFFFAOYSA-N 0.000 description 2
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RJUCIROUEDJQIB-GQCTYLIASA-N (6e)-octa-1,6-diene Chemical compound C\C=C\CCCC=C RJUCIROUEDJQIB-GQCTYLIASA-N 0.000 description 1
WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
PXGZQGDTEZPERC-UHFFFAOYSA-N 1,4-cyclohexanedicarboxylic acid Chemical compound OC(=O)C1CCC(C(O)=O)CC1 PXGZQGDTEZPERC-UHFFFAOYSA-N 0.000 description 1
125000001140 1,4-phenylene group Chemical group [H]C1=C([H])C([*:2])=C([H])C([H])=C1[*:1] 0.000 description 1
WKUVMNNFHURAPU-UHFFFAOYSA-N 1-(3,5-diethyl-2-methylphenyl)sulfonyl-3,5-diethyl-2-methylbenzene Chemical compound CCC1=CC(CC)=C(C)C(S(=O)(=O)C=2C(=C(CC)C=C(CC)C=2)C)=C1 WKUVMNNFHURAPU-UHFFFAOYSA-N 0.000 description 1
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UKGUOWQREAMCDW-UHFFFAOYSA-N 1-methoxy-2-[(2-methoxy-5-nitrophenyl)methyl]-4-nitrobenzene Chemical compound COC1=CC=C([N+]([O-])=O)C=C1CC1=CC([N+]([O-])=O)=CC=C1OC UKGUOWQREAMCDW-UHFFFAOYSA-N 0.000 description 1
DGPGVLIQUWUVIT-UHFFFAOYSA-N 1-methoxy-2-[1-(2-methoxyphenyl)ethyl]benzene Chemical compound COC1=CC=CC=C1C(C)C1=CC=CC=C1OC DGPGVLIQUWUVIT-UHFFFAOYSA-N 0.000 description 1
BXINIXQKBCSKKR-UHFFFAOYSA-N 1-phenylhexylbenzene Chemical compound C=1C=CC=CC=1C(CCCCC)C1=CC=CC=C1 BXINIXQKBCSKKR-UHFFFAOYSA-N 0.000 description 1
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235000007164 Oryza sativa Nutrition 0.000 description 1
ALQSHHUCVQOPAS-UHFFFAOYSA-N Pentane-1,5-diol Chemical compound OCCCCCO ALQSHHUCVQOPAS-UHFFFAOYSA-N 0.000 description 1
YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 description 1
241000282887 Suidae Species 0.000 description 1
241000620457 Telestes souffia Species 0.000 description 1
241001504592 Trachurus trachurus Species 0.000 description 1
239000012963 UV stabilizer Substances 0.000 description 1
LEHOTFFKMJEONL-UHFFFAOYSA-N Uric Acid Chemical compound N1C(=O)NC(=O)C2=C1NC(=O)N2 LEHOTFFKMJEONL-UHFFFAOYSA-N 0.000 description 1
TVWHNULVHGKJHS-UHFFFAOYSA-N Uric acid Natural products N1C(=O)NC(=O)C2NC(=O)NC21 TVWHNULVHGKJHS-UHFFFAOYSA-N 0.000 description 1
239000012190 activator Substances 0.000 description 1
239000000654 additive Substances 0.000 description 1
239000001361 adipic acid Substances 0.000 description 1
235000011037 adipic acid Nutrition 0.000 description 1
150000007933 aliphatic carboxylic acids Chemical class 0.000 description 1
150000001336 alkenes Chemical class 0.000 description 1
125000005250 alkyl acrylate group Chemical group 0.000 description 1
125000003282 alkyl amino group Chemical group 0.000 description 1
125000002877 alkyl aryl group Chemical group 0.000 description 1
238000004458 analytical method Methods 0.000 description 1
239000003963 antioxidant agent Substances 0.000 description 1
230000003078 antioxidant effect Effects 0.000 description 1
239000002216 antistatic agent Substances 0.000 description 1
238000000149 argon plasma sintering Methods 0.000 description 1
230000001588 bifunctional effect Effects 0.000 description 1
IFVTZJHWGZSXFD-UHFFFAOYSA-N biphenylene Chemical group C1=CC=C2C3=CC=CC=C3C2=C1 IFVTZJHWGZSXFD-UHFFFAOYSA-N 0.000 description 1
229940106691 bisphenol a Drugs 0.000 description 1
239000001273 butane Substances 0.000 description 1
KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
XSXWYGABGYBZRM-UHFFFAOYSA-N carbonic acid;4-[2-(4-hydroxyphenyl)propan-2-yl]phenol Chemical compound OC(O)=O.C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 XSXWYGABGYBZRM-UHFFFAOYSA-N 0.000 description 1
125000002843 carboxylic acid group Chemical group 0.000 description 1
230000003197 catalytic effect Effects 0.000 description 1
239000003153 chemical reaction reagent Substances 0.000 description 1
239000004927 clay Substances 0.000 description 1
150000001875 compounds Chemical class 0.000 description 1
238000007796 conventional method Methods 0.000 description 1
XCJYREBRNVKWGJ-UHFFFAOYSA-N copper(II) phthalocyanine Chemical compound [Cu+2].C12=CC=CC=C2C(N=C2[N-]C(C3=CC=CC=C32)=N2)=NC1=NC([C]1C=CC=CC1=1)=NC=1N=C1[C]3C=CC=CC3=C2[N-]1 XCJYREBRNVKWGJ-UHFFFAOYSA-N 0.000 description 1
238000005859 coupling reaction Methods 0.000 description 1
WYHYNUWZLKTEEY-UHFFFAOYSA-N cyclobutane-1,3-dicarboxylic acid Chemical compound OC(=O)C1CC(C(O)=O)C1 WYHYNUWZLKTEEY-UHFFFAOYSA-N 0.000 description 1
ZXJWWZPUERUHLC-UHFFFAOYSA-N cycloheptane-1,4-diol Chemical compound OC1CCCC(O)CC1 ZXJWWZPUERUHLC-UHFFFAOYSA-N 0.000 description 1
UVJHQYIOXKWHFD-UHFFFAOYSA-N cyclohexa-1,4-diene Chemical compound C1C=CCC=C1 UVJHQYIOXKWHFD-UHFFFAOYSA-N 0.000 description 1
125000004956 cyclohexylene group Chemical group 0.000 description 1
125000000640 cyclooctyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C([H])([H])C1([H])[H] 0.000 description 1
ASJCSAKCMTWGAH-UHFFFAOYSA-N cyclopentane-1,2-dicarboxylic acid Chemical compound OC(=O)C1CCCC1C(O)=O ASJCSAKCMTWGAH-UHFFFAOYSA-N 0.000 description 1
IKJFYINYNJYDTA-UHFFFAOYSA-N dibenzothiophene sulfone Chemical compound C1=CC=C2S(=O)(=O)C3=CC=CC=C3C2=C1 IKJFYINYNJYDTA-UHFFFAOYSA-N 0.000 description 1
125000004188 dichlorophenyl group Chemical group 0.000 description 1
125000005442 diisocyanate group Chemical group 0.000 description 1
HBGGXOJOCNVPFY-UHFFFAOYSA-N diisononyl phthalate Chemical compound CC(C)CCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCC(C)C HBGGXOJOCNVPFY-UHFFFAOYSA-N 0.000 description 1
239000000539 dimer Substances 0.000 description 1
238000006471 dimerization reaction Methods 0.000 description 1
OREAFAJWWJHCOT-UHFFFAOYSA-N dimethylmalonic acid Chemical compound OC(=O)C(C)(C)C(O)=O OREAFAJWWJHCOT-UHFFFAOYSA-N 0.000 description 1
239000006185 dispersion Substances 0.000 description 1
238000009826 distribution Methods 0.000 description 1
238000010292 electrical insulation Methods 0.000 description 1
229940096118 ella Drugs 0.000 description 1
125000005670 ethenylalkyl group Chemical group 0.000 description 1
238000011156 evaluation Methods 0.000 description 1
230000008020 evaporation Effects 0.000 description 1
238000001704 evaporation Methods 0.000 description 1
239000000945 filler Substances 0.000 description 1
239000003063 flame retardant Substances 0.000 description 1
YLQWCDOCJODRMT-UHFFFAOYSA-N fluoren-9-one Chemical compound C1=CC=C2C(=O)C3=CC=CC=C3C2=C1 YLQWCDOCJODRMT-UHFFFAOYSA-N 0.000 description 1
238000007306 functionalization reaction Methods 0.000 description 1
239000003365 glass fiber Substances 0.000 description 1
229930195712 glutamate Natural products 0.000 description 1
239000008187 granular material Substances 0.000 description 1
239000001046 green dye Substances 0.000 description 1
239000001056 green pigment Substances 0.000 description 1
XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 1
229930195733 hydrocarbon Natural products 0.000 description 1
150000002430 hydrocarbons Chemical class 0.000 description 1
229910052739 hydrogen Inorganic materials 0.000 description 1
239000001257 hydrogen Substances 0.000 description 1
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
150000003949 imides Chemical class 0.000 description 1
239000012442 inert solvent Substances 0.000 description 1
QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
150000003951 lactams Chemical class 0.000 description 1
MOUPNEIJQCETIW-UHFFFAOYSA-N lead chromate Chemical compound [Pb+2].[O-][Cr]([O-])(=O)=O MOUPNEIJQCETIW-UHFFFAOYSA-N 0.000 description 1
239000000314 lubricant Substances 0.000 description 1
238000003754 machining Methods 0.000 description 1
230000014759 maintenance of location Effects 0.000 description 1
150000002691 malonic acids Chemical class 0.000 description 1
FRVOOSTVCDXSRG-UHFFFAOYSA-N methanediimine;3,5,5-trimethylcyclohex-2-en-1-one Chemical compound N=C=N.CC1=CC(=O)CC(C)(C)C1 FRVOOSTVCDXSRG-UHFFFAOYSA-N 0.000 description 1
125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 1
239000006082 mold release agent Substances 0.000 description 1
FZLUWDXMHJPGBS-UHFFFAOYSA-N n-(3-aminopropyl)prop-2-enamide Chemical compound NCCCNC(=O)C=C FZLUWDXMHJPGBS-UHFFFAOYSA-N 0.000 description 1
IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 1
KYTZHLUVELPASH-UHFFFAOYSA-N naphthalene-1,2-dicarboxylic acid Chemical compound C1=CC=CC2=C(C(O)=O)C(C(=O)O)=CC=C21 KYTZHLUVELPASH-UHFFFAOYSA-N 0.000 description 1
WPUMVKJOWWJPRK-UHFFFAOYSA-N naphthalene-2,7-dicarboxylic acid Chemical compound C1=CC(C(O)=O)=CC2=CC(C(=O)O)=CC=C21 WPUMVKJOWWJPRK-UHFFFAOYSA-N 0.000 description 1
IFSXZLJQEKGQAF-UHFFFAOYSA-M nuclear fast red Chemical compound [Na+].O=C1C2=CC=CC=C2C(=O)C2=C1C(O)=C(S([O-])(=O)=O)C(O)=C2N IFSXZLJQEKGQAF-UHFFFAOYSA-M 0.000 description 1
239000002667 nucleating agent Substances 0.000 description 1
ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
238000002103 osmometry Methods 0.000 description 1
150000002918 oxazolines Chemical class 0.000 description 1
150000002924 oxiranes Chemical class 0.000 description 1
125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 description 1
OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical group OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 description 1
239000004014 plasticizer Substances 0.000 description 1
229920002239 polyacrylonitrile Polymers 0.000 description 1
238000006116 polymerization reaction Methods 0.000 description 1
229920001296 polysiloxane Polymers 0.000 description 1
238000012545 processing Methods 0.000 description 1
239000003380 propellant Substances 0.000 description 1
WQGWDDDVZFFDIG-UHFFFAOYSA-N pyrogallol Chemical class OC1=CC=CC(O)=C1O WQGWDDDVZFFDIG-UHFFFAOYSA-N 0.000 description 1
229920005604 random copolymer Polymers 0.000 description 1
239000011347 resin Substances 0.000 description 1
229920005989 resin Polymers 0.000 description 1
PYWVYCXTNDRMGF-UHFFFAOYSA-N rhodamine B Chemical compound [Cl-].C=12C=CC(=[N+](CC)CC)C=C2OC2=CC(N(CC)CC)=CC=C2C=1C1=CC=CC=C1C(O)=O PYWVYCXTNDRMGF-UHFFFAOYSA-N 0.000 description 1
235000009566 rice Nutrition 0.000 description 1
238000005096 rolling process Methods 0.000 description 1
239000011265 semifinished product Substances 0.000 description 1
238000010583 slow cooling Methods 0.000 description 1
AXXJTNXVUHVOJW-UHFFFAOYSA-M sodium;5-pentan-2-yl-5-prop-2-enylpyrimidin-3-ide-2,4,6-trione Chemical compound [Na+].CCCC(C)C1(CC=C)C(=O)NC(=O)[N-]C1=O AXXJTNXVUHVOJW-UHFFFAOYSA-M 0.000 description 1
239000007787 solid Substances 0.000 description 1
230000003381 solubilizing effect Effects 0.000 description 1
229920003048 styrene butadiene rubber Polymers 0.000 description 1
235000011044 succinic acid Nutrition 0.000 description 1
150000003444 succinic acids Chemical class 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
229910052714 tellurium Inorganic materials 0.000 description 1
BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 description 1
239000012815 thermoplastic material Substances 0.000 description 1
GWEVSGVZZGPLCZ-UHFFFAOYSA-N titanium dioxide Inorganic materials O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
238000004448 titration Methods 0.000 description 1
DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 1
125000003944 tolyl group Chemical group 0.000 description 1
238000005809 transesterification reaction Methods 0.000 description 1
MGMXGCZJYUCMGY-UHFFFAOYSA-N tris(4-nonylphenyl) phosphite Chemical compound C1=CC(CCCCCCCCC)=CC=C1OP(OC=1C=CC(CCCCCCCCC)=CC=1)OC1=CC=C(CCCCCCCCC)C=C1 MGMXGCZJYUCMGY-UHFFFAOYSA-N 0.000 description 1
OOLLAFOLCSJHRE-ZHAKMVSLSA-N ulipristal acetate Chemical compound C1=CC(N(C)C)=CC=C1[C@@H]1C2=C3CCC(=O)C=C3CC[C@H]2[C@H](CC[C@]2(OC(C)=O)C(C)=O)[C@]2(C)C1 OOLLAFOLCSJHRE-ZHAKMVSLSA-N 0.000 description 1
229940116269 uric acid Drugs 0.000 description 1
125000005023 xylyl group Chemical group 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L67/00—Compositions of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Compositions of derivatives of such polymers
- C08L67/02—Polyesters derived from dicarboxylic acids and dihydroxy compounds
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L69/00—Compositions of polycarbonates; Compositions of derivatives of polycarbonates
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L51/00—Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers
- C08L51/04—Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers grafted on to rubbers

Landscapes

Chemical & Material Sciences (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Organic Chemistry (AREA)
Compositions Of Macromolecular Compounds (AREA)

JP6522157A 1993-04-05 1994-03-23 高耐衝撃性ポリエステル／ポリカーボネート・ブレンド Pending JPH08508529A (ja)

Applications Claiming Priority (3)

Application Number	Priority Date	Filing Date	Title
US08/043,945 US5283285A (en)	1993-04-05	1993-04-05	High impact polyester/polycarbonate blends
US08/043,945		1993-04-05
PCT/US1994/003120 WO1994022955A1 (fr)	1993-04-05	1994-03-23	Melange de polyesters et de polycarbonates a haute resistance a l'impact

Publications (1)

Publication Number	Publication Date
JPH08508529A true JPH08508529A (ja)	1996-09-10

Family

ID=21929730

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP6522157A Pending JPH08508529A (ja)	1993-04-05	1994-03-23	高耐衝撃性ポリエステル／ポリカーボネート・ブレンド

Country Status (5)

Country	Link
US (1)	US5283285A (fr)
EP (1)	EP0693094A1 (fr)
JP (1)	JPH08508529A (fr)
CA (1)	CA2155649A1 (fr)
WO (1)	WO1994022955A1 (fr)

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US5523351A (en) *	1991-10-18	1996-06-04	The Goodyear Tire & Rubber Company	Compatibilized polymeric systems
EP0828793B1 (fr) *	1995-06-02	1999-04-28	Eastman Chemical Company	Polyesters d'acide 2,6-naphtalenedicarboxylique presentant une stabilite hydrolitique amelioree
US6100307A (en) *	1998-03-17	2000-08-08	Shell Oil Company	Compositions of polycondensed branched polyester polymers and aromatic polycarbonates, and the closed cell polymer foams made therefrom
WO2002060855A2 (fr) *	2000-12-28	2002-08-08	General Electric Company	Procede de preparation de polycarbonate
US6653434B2 (en)	2000-12-29	2003-11-25	General Electric Company	Process for the production of polycarbonate
US6525128B2 (en) *	2001-02-01	2003-02-25	The Goodyear Tire & Rubber Company	Composition of organophosphite, isobutylene copolymer and silica and tire thereof
US6515063B2 (en) *	2001-02-01	2003-02-04	The Goodyear Tire & Rubber Company	Tire having colored tread
US6583210B2 (en) *	2001-02-01	2003-06-24	The Goodyear Tire & Rubber Company	Tire having tread with co-extruded non-black colored overlay
US20030120025A1 (en) *	2001-09-07	2003-06-26	Brack Hans Peter	Process for the production of polycarbonate
CN101942182B (zh) *	2004-09-17	2012-05-23	东丽株式会社	树脂组合物和由其形成的成型品
DE102007040927A1 (de) *	2007-08-30	2009-03-05	Bayer Materialscience Ag	Verfahren zur Herstellung schlagzähmodifizierter gefüllter Polycarbonat-Zusammensetzungen

Family Cites Families (12)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GB1208585A (en) *	1967-12-11	1970-10-14	Ici Ltd	Polyester compositions
CA1056985A (fr) *	1975-03-17	1979-06-19	Celanese Corporation	Polyesters a extruder
US4172859A (en) *	1975-05-23	1979-10-30	E. I. Du Pont De Nemours And Company	Tough thermoplastic polyester compositions
US4096202A (en) *	1976-06-09	1978-06-20	Rohm And Haas Company	Impact modified poly(alkylene terephthalates)
JPS5966448A (ja) *	1982-10-07	1984-04-14	Mitsui Petrochem Ind Ltd	熱可塑性樹脂組成物
JPS61235455A (ja) *	1985-04-10	1986-10-20	Polyplastics Co	熱可塑性ポリエステル組成物
JPS60210659A (ja) *	1984-04-04	1985-10-23	Polyplastics Co	耐熱水性に優れたポリエステル組成物
US4879328A (en) *	1987-05-18	1989-11-07	Toray Industries	Aromatic polyester composition and process for producing the same
JPH01282256A (ja) *	1988-05-09	1989-11-14	Mitsubishi Gas Chem Co Inc	新規な耐衝撃性樹脂組成物
WO1989011507A1 (fr) *	1988-05-26	1989-11-30	Allied-Signal Inc.	Melange greffe d'un elastomere et d'un polyester thermoplastique
JPH0347844A (ja) *	1989-04-12	1991-02-28	Tonen Corp	ポリプロピレン―ポリエステルグラフト共重合体及びその製造方法
WO1992014787A1 (fr) *	1991-02-26	1992-09-03	The Dow Chemical Company	Melanges de compositons de moulage thermoplastique contenant des resines epoxy

1993
- 1993-04-05 US US08/043,945 patent/US5283285A/en not_active Expired - Lifetime
1994
- 1994-03-23 CA CA002155649A patent/CA2155649A1/fr not_active Abandoned
- 1994-03-23 JP JP6522157A patent/JPH08508529A/ja active Pending
- 1994-03-23 EP EP94913941A patent/EP0693094A1/fr not_active Withdrawn
- 1994-03-23 WO PCT/US1994/003120 patent/WO1994022955A1/fr not_active Ceased

Also Published As

Publication number	Publication date
EP0693094A1 (fr)	1996-01-24
CA2155649A1 (fr)	1994-10-13
WO1994022955A1 (fr)	1994-10-13
US5283285A (en)	1994-02-01

Publication	Publication Date	Title
JP2744138B2 (ja)	1998-04-28	脂肪族ポリアミドと芳香族ポリアミド・オリゴマーを含んで成る改善された耐湿性を有するポリアミド組成物
US4292233A (en)	1981-09-29	High-impact polybutylene terephthalate
US4231922A (en)	1980-11-04	Impact modified polyarylate blends
JPH01144417A (ja)	1989-06-06	ポリエーテルエステルアミドおよび熱可塑性樹脂組成物
JPH08508529A (ja)	1996-09-10	高耐衝撃性ポリエステル／ポリカーボネート・ブレンド
US3835098A (en)	1974-09-10	Process for improving thermoplastic elastomeric compositions
JPH0660268B2 (ja)	1994-08-10	ポリプロピレン系樹脂組成物
US5621040A (en)	1997-04-15	High impact polyester compositions
WO1997021745A1 (fr)	1997-06-19	Resine de polyolefine greffee et composition de resine thermoplastique la contenant
JP3899178B2 (ja)	2007-03-28	難燃性樹脂組成物
JPS63275659A (ja)	1988-11-14	末端基が制御されたポリアミド樹脂を含む熱可塑性ブレンド
JPS62187760A (ja)	1987-08-17	非晶質ポリアミドを含有する熱可塑性ブレンド
JP2011256222A (ja)	2011-12-22	ポリグリコール酸樹脂組成物
CA1296446C (fr)	1992-02-25	Addition de polyhydroxyether a des melanges de polyarylate et de polyamide
US20060036037A1 (en)	2006-02-16	Thermoplastic molding compositions
JPH0621222B2 (ja)	1994-03-23	樹脂組成物
JP3270147B2 (ja)	2002-04-02	ポリカーボネート系樹脂組成物
JP2001115036A (ja)	2001-04-24	難燃性ポリカーボネート系樹脂組成物
JPS61215647A (ja)	1986-09-25	耐熱耐衝撃性樹脂組成物
JPH032264A (ja)	1991-01-08	イソシアネート変性樹脂組成物
JPH01256560A (ja)	1989-10-13	主鎖にエステル結合及び／又はカーボネート結合を有する熱可塑性樹脂組成物
JPH0557302B2 (fr)	1993-08-23
JPH05117503A (ja)	1993-05-14	熱可塑性樹脂組成物
JPH02218738A (ja)	1990-08-31	樹脂組成物
JP3257888B2 (ja)	2002-02-18	熱可塑性樹脂組成物